{"title":"两种水通道蛋白LcPIP1;4和LcPIP1;4a协同调节常绿多年生荔枝(litchi chinensis Sonn.)顶芽的休眠。","authors":"Xue Tian, Zhi-Qun Zhong, Yu Qi, Meng-Meng Ma, Ming-Chao Yang, Dong-Cheng Li, Fang-Yi Zhang, Hui-Cong Wang, Ji-Yuan Shen, Ren-Fang Zeng, Xu-Ming Huang","doi":"10.1093/hr/uhaf122","DOIUrl":null,"url":null,"abstract":"Although extensively studied in various plants, the roles of aquaporin proteins in litchi remain unclear. In this study, low moisture content was observed in the dormant terminal buds of litchi. Transcriptome analysis revealed that two aquaporin genes, PLASMA MEMBRANE INTRINSIC PROTEIN 1;4 (LcPIP1;4) and LcPIP1;5, could be remarkably inhibited by exogenous ethylene (ETH), which also reduced the moisture content of litchi buds. Quantitative real-time PCR assays indicated that LcPIP1;4 expression was relatively elevated in the dormancy stage of litchi terminal buds. Inhibition of LcPIP1;4 in the buds of litchi during the growth stage delayed the onset of dormancy, resulting in a significantly reduced dormancy rate and increased moisture content. Further study indicated that LcPIP1;4 interacts with LcPIP1;4a, and they are capable of self-interaction. Silencing of LcPIP1;4a in litchi buds resulted in a phenotype consistent with silencing of LcPIP1;4. Additionally, simultaneous silencing of both LcPIP1;4 and LcPIP1;4a resulted in a more severe bud dormancy phenotype. Moreover, LcPIP1;4 was directly upregulated by LcRAP2.4. Silencing of LcRAP2.4 also delayed the onset of dormancy in litchi terminal buds, which is regulated by LcSVP2. ETH treatment at 1000 mg/L significantly downregulated the expression of LcPIP1;4 and LcRAP2.4, but had no significant effect on LcPIP1;4a. In contrast, ABA treatment at 200 mg/L significantly upregulated the expression of LcPIP1;4, LcPIP1;4a, and LcRAP2.4. Combined treatment with ETH and ABA exerted a stronger inhibitory effect on the budbreak and upregulated LcPIP1;4 and LcRAP2.4 to lower degrees than ABA alone, suggesting that ABA reversed the inhibitory effect of ETH on expression of LcPIP1;4 and LcRAP2.4. ABA treatment and combined treatment with ETH and ABA effectively reduced the moisture content of the terminal buds. These results demonstrate that LcRAP2,4, LcPIP1;4, and LcPIP1;4a play a vital role in dormancy onset of litchi terminal buds by regulating moisture levels.","PeriodicalId":13179,"journal":{"name":"Horticulture Research","volume":"14 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Two aquaporins, LcPIP1;4 and LcPIP1;4a, cooperatively regulate the onset of dormancy of the terminal buds in evergreen perennial litchi (Litchi chinensis Sonn.)\",\"authors\":\"Xue Tian, Zhi-Qun Zhong, Yu Qi, Meng-Meng Ma, Ming-Chao Yang, Dong-Cheng Li, Fang-Yi Zhang, Hui-Cong Wang, Ji-Yuan Shen, Ren-Fang Zeng, Xu-Ming Huang\",\"doi\":\"10.1093/hr/uhaf122\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Although extensively studied in various plants, the roles of aquaporin proteins in litchi remain unclear. In this study, low moisture content was observed in the dormant terminal buds of litchi. Transcriptome analysis revealed that two aquaporin genes, PLASMA MEMBRANE INTRINSIC PROTEIN 1;4 (LcPIP1;4) and LcPIP1;5, could be remarkably inhibited by exogenous ethylene (ETH), which also reduced the moisture content of litchi buds. Quantitative real-time PCR assays indicated that LcPIP1;4 expression was relatively elevated in the dormancy stage of litchi terminal buds. Inhibition of LcPIP1;4 in the buds of litchi during the growth stage delayed the onset of dormancy, resulting in a significantly reduced dormancy rate and increased moisture content. Further study indicated that LcPIP1;4 interacts with LcPIP1;4a, and they are capable of self-interaction. Silencing of LcPIP1;4a in litchi buds resulted in a phenotype consistent with silencing of LcPIP1;4. Additionally, simultaneous silencing of both LcPIP1;4 and LcPIP1;4a resulted in a more severe bud dormancy phenotype. Moreover, LcPIP1;4 was directly upregulated by LcRAP2.4. Silencing of LcRAP2.4 also delayed the onset of dormancy in litchi terminal buds, which is regulated by LcSVP2. ETH treatment at 1000 mg/L significantly downregulated the expression of LcPIP1;4 and LcRAP2.4, but had no significant effect on LcPIP1;4a. In contrast, ABA treatment at 200 mg/L significantly upregulated the expression of LcPIP1;4, LcPIP1;4a, and LcRAP2.4. Combined treatment with ETH and ABA exerted a stronger inhibitory effect on the budbreak and upregulated LcPIP1;4 and LcRAP2.4 to lower degrees than ABA alone, suggesting that ABA reversed the inhibitory effect of ETH on expression of LcPIP1;4 and LcRAP2.4. ABA treatment and combined treatment with ETH and ABA effectively reduced the moisture content of the terminal buds. These results demonstrate that LcRAP2,4, LcPIP1;4, and LcPIP1;4a play a vital role in dormancy onset of litchi terminal buds by regulating moisture levels.\",\"PeriodicalId\":13179,\"journal\":{\"name\":\"Horticulture Research\",\"volume\":\"14 1\",\"pages\":\"\"},\"PeriodicalIF\":8.7000,\"publicationDate\":\"2025-05-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Horticulture Research\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1093/hr/uhaf122\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Agricultural and Biological Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Horticulture Research","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1093/hr/uhaf122","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
Two aquaporins, LcPIP1;4 and LcPIP1;4a, cooperatively regulate the onset of dormancy of the terminal buds in evergreen perennial litchi (Litchi chinensis Sonn.)
Although extensively studied in various plants, the roles of aquaporin proteins in litchi remain unclear. In this study, low moisture content was observed in the dormant terminal buds of litchi. Transcriptome analysis revealed that two aquaporin genes, PLASMA MEMBRANE INTRINSIC PROTEIN 1;4 (LcPIP1;4) and LcPIP1;5, could be remarkably inhibited by exogenous ethylene (ETH), which also reduced the moisture content of litchi buds. Quantitative real-time PCR assays indicated that LcPIP1;4 expression was relatively elevated in the dormancy stage of litchi terminal buds. Inhibition of LcPIP1;4 in the buds of litchi during the growth stage delayed the onset of dormancy, resulting in a significantly reduced dormancy rate and increased moisture content. Further study indicated that LcPIP1;4 interacts with LcPIP1;4a, and they are capable of self-interaction. Silencing of LcPIP1;4a in litchi buds resulted in a phenotype consistent with silencing of LcPIP1;4. Additionally, simultaneous silencing of both LcPIP1;4 and LcPIP1;4a resulted in a more severe bud dormancy phenotype. Moreover, LcPIP1;4 was directly upregulated by LcRAP2.4. Silencing of LcRAP2.4 also delayed the onset of dormancy in litchi terminal buds, which is regulated by LcSVP2. ETH treatment at 1000 mg/L significantly downregulated the expression of LcPIP1;4 and LcRAP2.4, but had no significant effect on LcPIP1;4a. In contrast, ABA treatment at 200 mg/L significantly upregulated the expression of LcPIP1;4, LcPIP1;4a, and LcRAP2.4. Combined treatment with ETH and ABA exerted a stronger inhibitory effect on the budbreak and upregulated LcPIP1;4 and LcRAP2.4 to lower degrees than ABA alone, suggesting that ABA reversed the inhibitory effect of ETH on expression of LcPIP1;4 and LcRAP2.4. ABA treatment and combined treatment with ETH and ABA effectively reduced the moisture content of the terminal buds. These results demonstrate that LcRAP2,4, LcPIP1;4, and LcPIP1;4a play a vital role in dormancy onset of litchi terminal buds by regulating moisture levels.
期刊介绍:
Horticulture Research, an open access journal affiliated with Nanjing Agricultural University, has achieved the prestigious ranking of number one in the Horticulture category of the Journal Citation Reports ™ from Clarivate, 2022. As a leading publication in the field, the journal is dedicated to disseminating original research articles, comprehensive reviews, insightful perspectives, thought-provoking comments, and valuable correspondence articles and letters to the editor. Its scope encompasses all vital aspects of horticultural plants and disciplines, such as biotechnology, breeding, cellular and molecular biology, evolution, genetics, inter-species interactions, physiology, and the origination and domestication of crops.